Canonical Allele Identifier: PA2827484130
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2062820
ClinVar RCV Id: RCV002958031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336271.1:p.Leu314Val
CA76530288
NM_001349342.3:c.940C>G